All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06772 NDCAGF Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies 618571 AR - - INTS1 - -
06800 NEDCHS ?Neurodevelopmental disorder with cerebellar hypoplasia and spasticity 618572 AR - - INTS8 - -
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